CX26, CX30, CX31.1 and CX43 are the predominant connexins in human cornea [132,133], their mutation results in ocular disorders such as oculodentodigital dysplasia, produced by mutations in CX43 and KID syndrome related to CX26 mutations, where keratitis is a major pathology [73,134,135]. This evidence concerns the gene GJB2 and KID syndrome.